@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_head
{
this:
np:hasAssertion
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_assertion
;
np:hasProvenance
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_assertion
a
np:Assertion
.
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_provenance
a
np:Provenance
.
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_assertion
{
miriam-gene:26047
a
ncit:C16612
.
lld:C0028945
a
ncit:C7057
.
dgn-gda:DGNe6a97075a99f19afb7e47d621796cdb6
sio:SIO_000628
miriam-gene:26047
,
lld:C0028945
;
a
sio:SIO_001121
.
}
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_provenance
{
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_assertion
dcterms:description
"[In a set of 25 glioblastomas and 22 oligodendrogliomas, mutation analysis identified two additional samples with genetic alterations in the CASPR2 gene and all three identified genetic alterations are likely to reduce CASPR2 protein expression levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:20711234
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP401604.RAcPizPAT8-GHWwTAfxgxYhnsEwMVqsUeqZheMsG8BMKc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}